152 related articles for article (PubMed ID: 10688370)
1. Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis.
Arin MJ; Longley MA; Epstein EH; Rothnagel JA; Roop DR
Exp Dermatol; 2000 Feb; 9(1):16-9. PubMed ID: 10688370
[TBL] [Abstract][Full Text] [Related]
2. An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis.
Arin MJ; Longley MA; Küster W; Huber M; Hohl D; Rothnagel JA; Roop DR
Exp Dermatol; 1999 Apr; 8(2):124-7. PubMed ID: 10232403
[TBL] [Abstract][Full Text] [Related]
3. A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.
Müller FB; Huber M; Kinaciyan T; Hausser I; Schaffrath C; Krieg T; Hohl D; Korge BP; Arin MJ
Hum Mol Genet; 2006 Apr; 15(7):1133-41. PubMed ID: 16505000
[TBL] [Abstract][Full Text] [Related]
4. A novel substitution in keratin 10 in epidermolytic hyperkeratosis.
Arin MJ; Longley MA; Anton-Lamprecht I; Kurze G; Huber M; Hohl D; Rothnagel JA; Roop DR
J Invest Dermatol; 1999 Apr; 112(4):506-8. PubMed ID: 10201536
[TBL] [Abstract][Full Text] [Related]
5. Epidermolytic hyperkeratosis with polycyclic psoriasiform plaques resulting from a mutation in the keratin 1 gene.
Michael EJ; Schneiderman P; Grossman ME; Christiano AM
Exp Dermatol; 1999 Dec; 8(6):501-3. PubMed ID: 10597140
[TBL] [Abstract][Full Text] [Related]
6. Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.
Compton JG; DiGiovanna JJ; Santucci SK; Kearns KS; Amos CI; Abangan DL; Korge BP; McBride OW; Steinert PM; Bale SJ
Nat Genet; 1992 Jul; 1(4):301-5. PubMed ID: 1284546
[TBL] [Abstract][Full Text] [Related]
7. Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene cluster.
Pulkkinen L; Christiano AM; Knowlton RG; Uitto J
J Clin Invest; 1993 Jan; 91(1):357-61. PubMed ID: 7678607
[TBL] [Abstract][Full Text] [Related]
8. A keratin K10 gene mutation in a Japanese patient with epidermolytic hyperkeratosis.
Nomura K; Meng X; Umeki K; Tamai K; Sawamura D; Hashimoto I; Kikuchi T
Jpn J Hum Genet; 1997 Mar; 42(1):217-23. PubMed ID: 9184002
[TBL] [Abstract][Full Text] [Related]
9. A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis.
Rothnagel JA; Fisher MP; Axtell SM; Pittelkow MR; Anton-Lamprecht I; Huber M; Hohl D; Roop DR
Hum Mol Genet; 1993 Dec; 2(12):2147-50. PubMed ID: 7509230
[TBL] [Abstract][Full Text] [Related]
10. Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.
Sybert VP; Francis JS; Corden LD; Smith LT; Weaver M; Stephens K; McLean WH
Am J Hum Genet; 1999 Mar; 64(3):732-8. PubMed ID: 10053007
[TBL] [Abstract][Full Text] [Related]
11. Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens.
Rothnagel JA; Traupe H; Wojcik S; Huber M; Hohl D; Pittelkow MR; Saeki H; Ishibashi Y; Roop DR
Nat Genet; 1994 Aug; 7(4):485-90. PubMed ID: 7524919
[TBL] [Abstract][Full Text] [Related]
12. Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene.
Cserhalmi-Friedman PB; Squeo R; Gordon D; Garzon M; Schneiderman P; Grossman ME; Christiano AM
Clin Exp Dermatol; 2000 May; 25(3):241-3. PubMed ID: 10844506
[TBL] [Abstract][Full Text] [Related]
13. Epidermolytic hyperkeratosis.
Bale SJ; Compton JG; DiGiovanna JJ
Semin Dermatol; 1993 Sep; 12(3):202-9. PubMed ID: 7692917
[TBL] [Abstract][Full Text] [Related]
14. Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs.
Credille KM; Barnhart KF; Minor JS; Dunstan RW
Br J Dermatol; 2005 Jul; 153(1):51-8. PubMed ID: 16029326
[TBL] [Abstract][Full Text] [Related]
15. Keratin 1 and keratin 10 mutations causing epidermolytic hyperkeratosis in Chinese patients.
Sun XK; Ma LL; Xie YQ; Zhu XJ
J Dermatol Sci; 2002 Sep; 29(3):195-200. PubMed ID: 12234709
[TBL] [Abstract][Full Text] [Related]
16. A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma.
Joh GY; Traupe H; Metze D; Nashan D; Huber M; Hohl D; Longley MA; Rothnagel JA; Roop DR
J Invest Dermatol; 1997 Mar; 108(3):357-61. PubMed ID: 9036939
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE).
McLean WH; Eady RA; Dopping-Hepenstal PJ; McMillan JR; Leigh IM; Navsaria HA; Higgins C; Harper JI; Paige DG; Morley SM
J Invest Dermatol; 1994 Jan; 102(1):24-30. PubMed ID: 7507152
[TBL] [Abstract][Full Text] [Related]
18. Preferential sites in keratin 10 that are mutated in epidermolytic hyperkeratosis.
Chipev CC; Yang JM; DiGiovanna JJ; Steinert PM; Marekov L; Compton JG; Bale SJ
Am J Hum Genet; 1994 Feb; 54(2):179-90. PubMed ID: 7508181
[TBL] [Abstract][Full Text] [Related]
19. Characterization of an immortalized cell line from a patient with epidermolytic hyperkeratosis.
Chipev CC; Steinert PM; Woodworth CD
J Invest Dermatol; 1996 Mar; 106(3):385-90. PubMed ID: 8648165
[TBL] [Abstract][Full Text] [Related]
20. Epidermolytic hyperkeratosis: applied molecular genetics.
DiGiovanna JJ; Bale SJ
J Invest Dermatol; 1994 Mar; 102(3):390-4. PubMed ID: 7509838
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
